@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP229127.RAbNfDTbXYdSyVBEgIt2T9Nqivz_WSFiR_jY9f7UMcLcw
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP229127.RAbNfDTbXYdSyVBEgIt2T9Nqivz_WSFiR_jY9f7UMcLcw130_head
{
this:
np:hasAssertion
dgn-np:NP229127.RAbNfDTbXYdSyVBEgIt2T9Nqivz_WSFiR_jY9f7UMcLcw130_assertion
;
np:hasProvenance
dgn-np:NP229127.RAbNfDTbXYdSyVBEgIt2T9Nqivz_WSFiR_jY9f7UMcLcw130_provenance
;
np:hasPublicationInfo
dgn-np:NP229127.RAbNfDTbXYdSyVBEgIt2T9Nqivz_WSFiR_jY9f7UMcLcw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP229127.RAbNfDTbXYdSyVBEgIt2T9Nqivz_WSFiR_jY9f7UMcLcw130_assertion
a
np:Assertion
.
dgn-np:NP229127.RAbNfDTbXYdSyVBEgIt2T9Nqivz_WSFiR_jY9f7UMcLcw130_provenance
a
np:Provenance
.
dgn-np:NP229127.RAbNfDTbXYdSyVBEgIt2T9Nqivz_WSFiR_jY9f7UMcLcw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP229127.RAbNfDTbXYdSyVBEgIt2T9Nqivz_WSFiR_jY9f7UMcLcw130_assertion
{
miriam-gene:23600
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGN23050bbf4d41c0812e6bdc3ce0acb706
sio:SIO_000628
miriam-gene:23600
,
lld:C0677886
;
a
sio:SIO_001121
.
}
dgn-np:NP229127.RAbNfDTbXYdSyVBEgIt2T9Nqivz_WSFiR_jY9f7UMcLcw130_provenance
{
dgn-np:NP229127.RAbNfDTbXYdSyVBEgIt2T9Nqivz_WSFiR_jY9f7UMcLcw130_assertion
dcterms:description
"[Rapid amplification of cDNA ends (RACE) mapping revealed that the transcriptional start site of BORIS in human testis, DNMT deficient human cancer cells, and human epithelial ovarian cancer (EOC) tissues, is similar and lies within the 5' CpG island.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:18095639
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP229127.RAbNfDTbXYdSyVBEgIt2T9Nqivz_WSFiR_jY9f7UMcLcw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}